I. Introduction: Proper sample preparation is one of the most important
requirements in the analysis of powder samples by X-ray diffraction (XRD).
This statement is especially true for soils and clays that contain finely
divided colloids, which are poor reflectors of x-rays, as well as other types
of materials such as iron oxide coatings and organic materials that make
characterization by XRD more difficult. Sample preparation includes not
only the right sample treatments to remove undesirable substances, but
also appropriate techniques to obtain desirable particle size, orientation,
thickness, etc. Several excellent books are available that deal with
appropriate sample preparation techniques for clays and soils (Jackson
1979, Brindley and Brown 1980, Moore and Reynolds 1989, Bish 1992,
Iyengar 1997)

II. Sample preparation
1: Drying:
Soils and clays are dried before they are ground and separated into
various particle sizes.
2: Grinding:
Analysis of powders by XRD requires that they be extremely fine grained to
achieve good signal-to noise ratio (and avoid fluctuation in intensity), avoid
spottiness and minimize preferred orientation. Reduction of powders to
fine particles also insures enough particle participation in the diffraction
process. The recommended size range is around 1-5 uM (Klug and
Alexander 1974, Cullity 1978, Brindley, 1980), especially if quantification of
various phases is desired. For routine qualitative evaluation of mineral
components, the samples are usually ground to pass through a 325 mesh
sieve (45 uM). Grinding is accomplished either through hand grinding or in
a mechanical grinder. The effects of excessive grinding include lattice
distortion and possible formation of an amorphous layer (Beilby layer)
outside the grains.

III. Pretreatments:
The ground soil and clay sample may require certain pre-treatments before
they can be analyzed by XRD. This step is to remove undesirable coatings
and cements, either to improve the diffraction characteristics of the sample
or to promote dispersion during size fractionation. Relatively pure clay
samples may not require any of these pre-treatments. Soil samples, on the
other hand, will require most of these treatments.
The pre-treatment can be grouped into the following:

  1. Removal of soluble salts and carbonaceous cements
  2. Removal of organic matter
  3. Removal of sesquioxide coatings
  4. Removal of oil contamination

IV: Size separation:
Size ranges: Minerals occur in various size ranges. The USDA system of
size classification is shown below:

Very Coarse Sand              2.00 - 1.00 mm
Coarse Sand                      1.00 - 0.50
Medium Sand                      0.50 - 0.25
Fine Sand                0.25 - 0.10
Very Fine Sand           0.10 - 0.05
Coarse Silt              0.05 - 0.005
Fine Silt                0.005 - 0.002
Clay                   < 0.002

It is often necessary to fractionate soil and clay samples to one of these
size ranges to elucidate and quantify specific mineral species present.

Coarse size fractions are obtained either by wet or dry sieving through a
standard set of sieves. The fine fractions, starting from very fine sand, are
separated by a combination of wet sieving and gravity or centrifugal
sedimentation.

Optimum size: What is the optimum size range to study clay minerals?.
This choice depends on the types of clay mineral present. Generally,
samples are separated to less than 2 or 5 micrometers to examine various
clay minerals. Figure 1 shows the XRD patterns for four different size fine
fractions from a sandstone rock. In this sample, kaolinite and mica was
present even in 5 -50 uM range, and the delectability of smectite increased
with a decrease in size range examined.

Separation Techniques: The dispersed sample is wet sieved through 325
mesh sieve (~ 50 uM) to separate very fine sand. The suspension or
centrifuge method is then used to separate other fine (clay and silt)
fractions either by gravity sedimentation or centrifugation. The settling
times required to separate various size ranges are based on Stokes' law
and are presented in extensive nomographs and tables by Jackson (1979).

V. Slide preparation and Analysis:
Two important criteria to keep in mind while preparing slides for XRD
analysis are the amount of sample and orientation of crystallites.
Amount of sample: The amount of sample should be enough to produce
an "infinitely" thick sample (Brindley 1980, Moore and Reynolds 1989).
Infinitely thick sample is defined as that thickness of the sample that yields
optimum diffracted intensity. Increasing its thickness (by adding more
sample) will result in a negligible increase in diffracted intensity.
Orientation of crystallites: The type of mounts normally employed are
dictated by the nature of crystallite orientation required and can be grouped
into random or oriented mounts.
a: Random Mounts:
Random mounts are preferred when mineralogy of a whole soil or clay is
required. In this type of mount, particles are packed to assume different
orientations and insure reflections from various hkl planes. Types of
random mounts available include: Spray drying, Front-loading, Rear-
loading, Side-loading or drifting, and Vaseline coated. These methods are
described elsewhere.
b: Oriented Mounts:
Several methods are available to prepare oriented mounts. Some of the
methods available include: Slurry Mount. Centrifuge on tile, Suction on
Millipore


Ion Saturation: Why ion saturation? The (00l) spacing from an oriented clay
depends on the type of cations in the interlayer region. In nature, clays and
soils are saturated with various types of cations including Na+, Ca2+,
Mg2+, K+. It is easier, for proper identification, to make them monoionic.

Glycolation: For identification of expandable clay minerals, several organic
reagents are used for intercalation. The most commonly used solvents are
ethylene glycol (EG) and glycerol.
Heat Treatment: Clay mounts on ceramic substrates, Si crystals, silver
membranes or certain glass substrates can be heated to various
temperatures for the identification of mineral species. The temperatures
normally used are 120 - 150 C (overnight), 300 C ( 4 to 5 hrs) and 550 C ( 4
to 5 hrs).

VI. References:
  • Bish, D. L. and J. E. Post (1989) Modern Powder Diffraction.
    Reviews in Mineralogy Volume 20. Published by Mineralogical
    Society of America, Washington, D. C.

  • Brindley, G. W. and G. Brown (1980) Crystal structures of Clay
    Minerals and Their Identification. Mineralogical Society Monograph
    NO. 5. Mineralogical Society, London

  • Cullity B. D. (1978) Elements of X-ray Diffraction, 2nd Edition.
    Addison-Wesley Publishing Co. Menlo Park, CA.

  • Iyengar, S. S. (1997) Sample Preparation for Clays In Preparation of
    Specimens for X-ray Fluorescence and X-ray Diffractuion Analysis.
    Eds. V.E. Buhrke, R. Jenkins and D.K. Smith. Wiley-VCH, NY

  • Jackson, M. L. (1979) Soil Chemical Analysis -- Advanced Course.
    2nd Edition, Published by the Author, Madison, Wis. 53705

  • Klug H. P. and L. E. Alexander (1974) X-ray Diffraction Procedures.
    J. Wiley and Sons, Inc. New York. 996p

  • Kunze, G. W. 1965. Pretreatments for Mineralogical Analysis. In C.
    A. Black (ed) Methods of Soil Analysis. Part I. Physical and
    Mineralogical properties including statistics of measurement and
    sampling. Agronomy 9: 568-577. Am. Soc. of Agronomy, Madison,
    WI

  • Moore, D. M. and R. C. Reynolds, Jr. (1989) X-ray Diffraction and the
    Identification and Analysis of Clay Minerals. Oxford University Press,
    Oxford.


Technology of Materials
Analysis of Clays and Soils by XRD